Development and preliminary evaluation of an online educational video about whole-genome sequencing for research participants, patients, and the general public

por Sanderson, Saskia C., Suckiel, Sabrina A., Zweig, Micol, Bottinger, Erwin P., Jabs, Ethylin Wang, Richardson, Lynne D.
Publicado 2016

Genomic Screening Identifies Individuals at High Risk for Hereditary Transthyretin Amyloidosis

por Soper, Emily R., Suckiel, Sabrina A., Braganza, Giovanna T., Kontorovich, Amy R., Kenny, Eimear E., Abul-Husn, Noura S.
Publicado 2021

Psychological and behavioural impact of returning personal results from whole-genome sequencing: the HealthSeq project

por Sanderson, Saskia C, Linderman, Michael D, Suckiel, Sabrina A, Zinberg, Randi, Wasserstein, Melissa, Kasarskis, Andrew, Diaz, George A, Schadt, Eric E
Publicado 2017

Perspectives of diverse Spanish- and English-speaking patients on the clinical use of polygenic risk scores

por Suckiel, Sabrina A., Braganza, Giovanna T., Aguiñiga, Karla López, Odgis, Jacqueline A., Bonini, Katherine E., Kenny, Eimear E., Hamilton, Jada G., Abul-Husn, Noura S.
Publicado 2022

Motivations, concerns and preferences of personal genome sequencing research participants: Baseline findings from the HealthSeq project

por Sanderson, Saskia C, Linderman, Michael D, Suckiel, Sabrina A, Diaz, George A, Zinberg, Randi E, Ferryman, Kadija, Wasserstein, Melissa, Kasarskis, Andrew, Schadt, Eric E
Publicado 2016

Impacts of incorporating personal genome sequencing into graduate genomics education: a longitudinal study over three course years

por Linderman, Michael D., Sanderson, Saskia C., Bashir, Ali, Diaz, George A., Kasarskis, Andrew, Zinberg, Randi, Mahajan, Milind, Suckiel, Sabrina A., Zweig, Micol, Schadt, Eric E.
Publicado 2018

Preparing the next generation of genomicists: a laboratory-style course in medical genomics

por Linderman, Michael D., Bashir, Ali, Diaz, George A., Kasarskis, Andrew, Sanderson, Saskia C., Zinberg, Randi E., Mahajan, Milind, Shah, Hardik, Suckiel, Sabrina, Zweig, Micol, Schadt, Eric E.
Publicado 2015

Exome sequencing reveals a high prevalence of BRCA1 and BRCA2 founder variants in a diverse population-based biobank

por Abul-Husn, Noura S., Soper, Emily R., Odgis, Jacqueline A., Cullina, Sinead, Bobo, Dean, Moscati, Arden, Rodriguez, Jessica E., Loos, Ruth J. F., Cho, Judy H., Belbin, Gillian M., Suckiel, Sabrina A., Kenny, Eimear E.
Publicado 2019

“Is that something that should concern me?”: a qualitative exploration of parent understanding of their child’s genomic test results

por Watnick, Dana, Odgis, Jacqueline A., Suckiel, Sabrina A., Gallagher, Katie M., Teitelman, Nehama, Donohue, Katherine E., Gelb, Bruce D., Kenny, Eimear E., Wasserstein, Melissa P., Horowitz, Carol R., Dolan, Siobhan M., Bauman, Laurie J.
Publicado 2021

Implementing genomic screening in diverse populations

por Abul-Husn, Noura S., Soper, Emily R., Braganza, Giovanna T., Rodriguez, Jessica E., Zeid, Natasha, Cullina, Sinead, Bobo, Dean, Moscati, Arden, Merkelson, Amanda, Loos, Ruth J. F., Cho, Judy H., Belbin, Gillian M., Suckiel, Sabrina A., Kenny, Eimear E.
Publicado 2021

Genomic Sequencing Results Disclosure in Diverse and Medically Underserved Populations: Themes, Challenges, and Strategies from the CSER Consortium

por Suckiel, Sabrina A., O’Daniel, Julianne M., Donohue, Katherine E., Gallagher, Katie M., Gilmore, Marian J., Hendon, Laura G., Joseph, Galen, Lianoglou, Billie R., Mathews, Jennifer M., Norton, Mary E., Odgis, Jacqueline A., Poss, Alexis F., Rego, Shannon, Scollon, Sarah, Yip, Tiffany, Amendola, Laura M.
Publicado 2021

GenomeDiver: A platform for phenotype-guided medical genomic diagnosis.

por Pearson, Nathaniel M., Stolte, Christian, Shi, Kevin, Beren, Faygel, Abul-Husn, Noura S., Bertier, Gabrielle, Brown, Kaitlyn, Diaz, George A., Odgis, Jacqueline A., Suckiel, Sabrina A., Horowitz, Carol R., Wasserstein, Melissa, Gelb, Bruce D., Kenny, Eimear E., Gagnon, Charles, Jobanputra, Vaidehi, Bloom, Toby, Greally, John M.
Publicado 2021

The NYCKidSeq randomized controlled trial: Impact of GUÍA digitally enhanced genetic counseling in racially and ethnically diverse families

por Suckiel, Sabrina A., Kelly, Nicole R., Odgis, Jacqueline A., Gallagher, Katie M., Sebastin, Monisha, Bonini, Katherine E., Marathe, Priya N., Brown, Kaitlyn, Di Biase, Miranda, Ramos, Michelle A., Rodriguez, Jessica E., Scarimbolo, Laura, Insel, Beverly J., Ferar, Kathleen D.M., Zinberg, Randi E., Diaz, George A., Greally, John M., Abul-Husn, Noura S., Bauman, Laurie J., Gelb, Bruce D., Horowitz, Carol R., Wasserstein, Melissa P., Kenny, Eimear E.
Publicado 2023

Molecular diagnostic yield of genome sequencing versus targeted gene panel testing in racially and ethnically diverse pediatric patients

por Abul-Husn, Noura S., Marathe, Priya N., Kelly, Nicole R., Bonini, Katherine E., Sebastin, Monisha, Odgis, Jacqueline A., Abhyankar, Avinash, Brown, Kaitlyn, Di Biase, Miranda, Gallagher, Katie M., Guha, Saurav, Ioele, Nicolette, Okur, Volkan, Ramos, Michelle A., Rodriguez, Jessica E., Rehman, Atteeq U., Thomas-Wilson, Amanda, Edelmann, Lisa, Zinberg, Randi E., Diaz, George A., Greally, John M., Jobanputra, Vaidehi, Suckiel, Sabrina A., Horowitz, Carol R., Wasserstein, Melissa P., Kenny, Eimear E., Gelb, Bruce D.
Publicado 2023

GUÍA: a digital platform to facilitate result disclosure in genetic counseling

por Suckiel, Sabrina A., Odgis, Jaqueline A., Gallagher, Katie M., Rodriguez, Jessica E., Watnick, Dana, Bertier, Gabrielle, Sebastin, Monisha, Yelton, Nicole, Maria, Estefany, Lopez, Jessenia, Ramos, Michelle, Kelly, Nicole, Teitelman, Nehama, Beren, Faygel, Kaszemacher, Tom, Davis, Kojo, Laguerre, Irma, Richardson, Lynne D., Diaz, George A., Pearson, Nathaniel M., Ellis, Stephen B., Stolte, Christian, Robinson, Mimsie, Kovatch, Patricia, Horowitz, Carol R., Gelb, Bruce D., Greally, John M., Bauman, Laurie J., Zinberg, Randi E., Abul-Husn, Noura S., Wasserstein, Melissa P., Kenny, Eimear E.
Publicado 2021

The TeleKidSeq pilot study: incorporating telehealth into clinical care of children from diverse backgrounds undergoing whole genome sequencing

por Sebastin, Monisha, Odgis, Jacqueline A., Suckiel, Sabrina A., Bonini, Katherine E., Di Biase, Miranda, Brown, Kaitlyn, Marathe, Priya, Kelly, Nicole R., Ramos, Michelle A., Rodriguez, Jessica E., Aguiñiga, Karla López, Lopez, Jessenia, Maria, Estefany, Rodriguez, Michelle A., Yelton, Nicole M., Cunningham-Rundles, Charlotte, Gallagher, Katie, McDonald, Thomas V., McGoldrick, Patricia E., Robinson, Mimsie, Rubinstein, Arye, Shulman, Lisa H., Wolf, Steven M., Yozawitz, Elissa, Zinberg, Randi E., Abul-Husn, Noura S., Bauman, Laurie J., Diaz, George A., Ferket, Bart S., Greally, John M., Jobanputra, Vaidehi, Gelb, Bruce D., Horowitz, Carol R., Kenny, Eimear E., Wasserstein, Melissa P.
Publicado 2023

The NYCKidSeq project: study protocol for a randomized controlled trial incorporating genomics into the clinical care of diverse New York City children

por Odgis, Jacqueline A., Gallagher, Katie M., Suckiel, Sabrina A., Donohue, Katherine E., Ramos, Michelle A., Kelly, Nicole R., Bertier, Gabrielle, Blackburn, Christina, Brown, Kaitlyn, Fielding, Lena, Lopez, Jessenia, Aguiniga, Karla Lopez, Maria, Estefany, Rodriguez, Jessica E., Sebastin, Monisha, Teitelman, Nehama, Watnick, Dana, Yelton, Nicole M., Abhyankar, Avinash, Abul-Husn, Noura S., Baum, Aaron, Bauman, Laurie J., Beal, Jules C., Bloom, Toby, Cunningham-Rundles, Charlotte, Diaz, George A., Dolan, Siobhan, Ferket, Bart S., Jobanputra, Vaidehi, Kovatch, Patricia, McDonald, Thomas V., McGoldrick, Patricia E., Rhodes, Rosamond, Rinke, Michael L., Robinson, Mimsie, Rubinstein, Arye, Shulman, Lisa H., Stolte, Christian, Wolf, Steven M., Yozawitz, Elissa, Zinberg, Randi E., Greally, John M., Gelb, Bruce D., Horowitz, Carol R., Wasserstein, Melissa P., Kenny, Eimear E.
Publicado 2021

Correction to: The NYCKidSeq project: study protocol for a randomized controlled trial incorporating genomics into the clinical care of diverse New York City children

por Odgis, Jacqueline A., Gallagher, Katie M., Suckiel, Sabrina A., Donohue, Katherine E., Ramos, Michelle A., Kelly, Nicole R., Bertier, Gabrielle, Blackburn, Christina, Brown, Kaitlyn, Fielding, Lena, Lopez, Jessenia, Aguiniga, Karla Lopez, Maria, Estefany, Rodriguez, Jessica E., Sebastin, Monisha, Teitelman, Nehama, Watnick, Dana, Yelton, Nicole M., Abhyankar, Avinash, Abul-Husn, Noura S., Baum, Aaron, Bauman, Laurie J., Beal, Jules C., Bloom, Toby, Cunningham-Rundles, Charlotte, Diaz, George A., Dolan, Siobhan, Ferket, Bart S., Jobanputra, Vaidehi, Kovatch, Patricia, McDonald, Thomas V., McGoldrick, Patricia E., Rhodes, Rosamond, Rinke, Michael L., Robinson, Mimsie, Rubinstein, Arye, Shulman, Lisa H., Stolte, Christian, Wolf, Steven M., Yozawitz, Elissa, Zinberg, Randi E., Greally, John M., Gelb, Bruce D., Horowitz, Carol R., Wasserstein, Melissa P., Kenny, Eimear E.
Publicado 2021